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LIVE POLIO IRUS VACCINES

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338 Efficacy--Laboratory Evidence<br />

GROUP:<br />

TABLE 4.<br />

<strong>POLIO</strong> ANTIBODY STATUS AND SALK HISTORY<br />

922 LEDERLE EMPLOYEES & FAMILIES<br />

DOSE: NONE TO FOUR SALK SHOTS DATE: 1959-60<br />

NEGATIVE TOTAL I PERSONS WITH SALK SHOTS<br />

TO TYPE PERSONS NONE 1 OR 2 3 OR 4<br />

No. % I No. % No. % No. %<br />

0 441 47.8 269 41.1 61 53.5 111 72.0<br />

1 100 10.8 76 11.6 14 12.3 10 6.5<br />

3 129 13.9 90 13.7 19 16.7 20 12.9<br />

1 & 3 53 5.7 i 34 5.2 8 7.0 11 7.1<br />

2 58 6.3 52 7.9 4 3.5 2 1.3<br />

1 & 2 45 4.9 45 6.9 0 0 0 0<br />

2 & 3 37 4.0 36 5.5 1 .9 0 0<br />

1, 2 & 3 59 6.4 52 7.9 7 6.1 0 0<br />

TOTALS 1922 654 114 154<br />

TABLE 5. FREQUENCY OF SERONEGATIVES IN<br />

SALK-VACCINATES AND NON-VACCINATES<br />

NO. OF<br />

PERSONS<br />

654<br />

114<br />

154<br />

NO. OF SERONEGATIVES (%)<br />

SALK SHOTS<br />

TO TYPE<br />

1 2 3<br />

O 31.7 28.3 32.4<br />

1-2 25.4 10.5 30.7<br />

3+ 13.6 1.3 20.1<br />

cent for Types 1 and 2 and 97 per cent for Type<br />

3. Moreover, from 37 to 45 per cent of those who<br />

had pre-vaccination antibody titers in the range<br />

of 1:4 to 1:512 showed four-fold or greater booster<br />

responses.<br />

DISCUSSION<br />

The data summarized in the present report are<br />

essentially an extension of our earlier study of<br />

trivalent vaccine which began in May 1958 with<br />

the simultaneous feeding of three capsules, each<br />

containing one of the three poliovirus strains.2<br />

This initial test was followed by the feeding of a<br />

fluid vaccine that contained balanced amounts of<br />

each of the three types of virus.l The results of<br />

those efforts were such as to justify the hope that<br />

the oral vaccination procedure could be simplified<br />

and made more rapid and less expensive,<br />

without any appreciable sacrifice of either efficiency<br />

or safety. Results obtained since in more<br />

than 1,200 additional volunteers confirm the<br />

earlier findings and provide a substantial basis<br />

for the greatly expanded field trials that are now<br />

in progress.<br />

The 88 per cent over-all conversion rate of<br />

seronegatives to seropositives, obtained in the<br />

present trivalent oral vaccine study, is comparable<br />

to, or slightly better than, rates reported<br />

for the separate feeding of the same strains of<br />

virus in children in Minnesota (85 per cent),3<br />

Colombia (83 per cent),' and Cuba (85 per<br />

cent).2 It is noteworthy, too, that for the most<br />

part, these conversions are based on sera collected<br />

four to five weeks after a single feeding. The<br />

conversion rates for virus Types 1 and 3, epidemiologically<br />

the most important, were over 93

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